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(G11.3) Cerebellar ataxia with defective dna repair
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149 554 in individuals diagnosis cerebellar ataxia with defective dna repair confirmed
16 151 deaths with diagnosis cerebellar ataxia with defective dna repair
11% mortality rate associated with the disease cerebellar ataxia with defective dna repair
Diagnosis cerebellar ataxia with defective dna repair is diagnosed Men are 20.27% more likely than Women
89 937
Men receive the diagnosis cerebellar ataxia with defective dna repair
8 312 (9.2 %)Died from this diagnosis.
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59 617
Women receive the diagnosis cerebellar ataxia with defective dna repair
7 839 (13.1 %)Died from this diagnosis.
Risk Group for the Disease cerebellar ataxia with defective dna repair - Men aged 45-49 and Women aged 55-59
In Men diagnosis is most often set at age 0-94
Less common in men the disease occurs at Age 0-1, 95+Less common in women the disease occurs at Age 0-1, 90-95+
In Women diagnosis is most often set at age 0-89
Disease Features cerebellar ataxia with defective dna repair
Absence or low individual and public risk
Cerebellar ataxia with defective dna repair - what does this mean
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What happens during the disease - cerebellar ataxia with defective dna repair
Cerebellar ataxia with defective dna repair is a rare genetic disorder caused by a mutation in the dna repair gene, which affects the ability of the body to repair damaged dna. this leads to an accumulation of errors in the dna which can cause a variety of neurological symptoms, including ataxia (incoordination), muscle weakness, and difficulty with balance and coordination. the underlying cause of this disorder is thought to be a defect in the body's ability to repair damaged dna, leading to the accumulation of errors in the genetic code.
Clinical Pattern
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How does a doctor diagnose
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Treatment and Medical Assistance
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24 Days of Hospitalization Required
Average Time for Outpatient Care Not Established
Cerebellar ataxia with defective dna repair - Prevention
The best way to prevent cerebellar ataxia with defective dna repair is to maintain a healthy lifestyle. this includes eating a balanced diet, exercising regularly, avoiding smoking and excessive alcohol consumption, and getting regular check-ups with your doctor. additionally, genetic counseling may be beneficial for those with a family history of the disease.